Abstract
Follicular dendritic-cell sarcoma (FDCS) is a rare and recalcitrant disease. In the present study, a patient-derived orthotopic xenograft (PDOX) mouse model of FDCS was established in the biceps muscle of nude mice. The FDCS PDOX was resistant to both doxorubicin (DOX) and NVP-BEZ235, dactolisib (BEZ) an experimental agent which is a dual pan-phosphoinositide 3-kinase-mammalian target of rapamycin inhibitor. However, in contrast to DOX and BEZ, the FDCS PDOX was sensitive to the tumor-targeting bacterial strain, Salmonella typhimurium A1-R (S. typhimurium A1-R). The combination of S. typhimurium A1-R and either DOX or BEZ did not increase the antitumor efficacy of S. typhimurium A1-R, indicating that DOX and BEZ were not active in this PDOX model. The efficacy of S. typhimurium A1-R in this recalcitrant FDCS gives strong impetus to move bacterial therapy to clinical trials for this disease. The findings of the present study are of particular importance since it demonstrates that S. typhimurium A1-R is effective in a PDOX model of FDCS established from a patient who failed DOX therapy.
Original language | English |
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Pages (from-to) | 33046-33054 |
Number of pages | 9 |
Journal | Oncotarget |
Volume | 7 |
Issue number | 22 |
DOIs | |
Publication status | Published - 2016 May 31 |
Externally published | Yes |
Keywords
- Doxorubicin
- GFP
- Nude mice
- PDOX
- Salmonella typhimurium A1-R
- Sarcoma
- Soft-tissue
- Tumor-targeting
ASJC Scopus subject areas
- Oncology